Dose Requirements of Remifentanil Used for Intubation in Non-Paralyzed Chinese Children

Clinical research of remifentanil’s ED50 and ED95 with Standard dose of propofol of the time in children with non-muscle relaxant intubation under general anesthesia

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-ONC-13003275

Enrollment

Unknown

Registered

2013-05-16

Start date

2012-01-01

Completion date

Unknown

Last updated

2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Disease

Interventions

research group:different doses of remifentanil

Eligibility

Sex/Gender

All

Age

3 Years to 9 Years

Inclusion criteria

Inclusion criteria: a total of 47 children were enrolled. All children were of the American Society of Anesthesiologists (ASA) Class I~II status

Exclusion criteria

Exclusion criteria: indications of a possible difficult airway

Design outcomes

Primary

Measure	Time frame
Grades of intubation condition;	—

Countries

China

Contacts

Public ContactQingquan Lian

lianqingquanmz@163.com+86 13957713889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026